反式激活crRNA
清脆的
核酸酶
核糖
Cas9
核糖核酸
核酸
计算生物学
引导RNA
DNA
化学
基因组编辑
生物化学
合理设计
限制
脱氧核酶
生物
突变
寡核苷酸
化学生物学
机制(生物学)
核酶
遗传学
基因
酶
DNA损伤
核酸结构
CRISPR干扰
化学改性
SOS响应
细胞生物学
聚ADP核糖聚合酶
作者
Adrian A Pater,Halle M Barber,Sruthi Sudhakar,Ramadevi Chilamkurthy,Sunit K Jana,Mansi A Parasrampuria,Michael S Bosmeny,Jacob A Graczyk-Marrs,Seth B Eddington,Cole A Blazier,Leonora Abdullahu,Elise Malek-Adamian,Christopher L Barkau,Daniel O'Reilly,Sergey Korolev,P I Pradeepkumar,Masad J Damha,Keith T Gagnon
标识
DOI:10.64898/2026.01.26.701763
摘要
Advanced CRISPR-based therapies benefit from CRISPR RNA (crRNA) with high nuclease resistance and enhanced drug-like properties, which is primarily achieved through chemical replacement of the RNA ribose moiety. However, for gene editing enzymes like CRISPR-Cas9 a handful of residues cannot be replaced with chemical ribose analogues, limiting the scope of therapeutic strategies. The mechanism underlying this restriction has remained unclear. Here, using nucleic acid chemistry, biochemistry, cryo-EM, and molecular dynamics simulations, we show that the ribose 2'-hydroxyl group at specific crRNA residues is required to achieve a conformational state competent for Cas9 target DNA binding. Based on the mechanistic principles uncovered, we combined site-specific phosphorothioate linkage chemistry with ribose replacement chemistry to restore binding and activity, resulting in high Cas9 editing efficiency and fidelity with a ribose-free crRNA. This study offers novel mechanistic insight and crRNAs with full chemical stabilization, making rational design of guide RNAs with complete nuclease protection for CRISPR-based medicines possible.
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